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Acute myeloid leukemia with 11q23 abnormalities

MONDO:0020317

An acute myeloid leukemia associated with t(9;11)(p22.3;q23.3) and MLLT3-KMT2A fusion protein expression. Morphologically it usually has monocytic features. It may present at any age but it is more commonly seen in children. Patients may present with disseminated intravascular coagulation.

Also known as: AML with 11q23 abnormalities, AML with t(9;11)(p22;q23); MLLT3-MLL, acute myeloid Leukaemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A, acute myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A, acute myeloid leukaemia with 11q23 (MLL) abnormalities, acute myeloid leukaemia with MLL abnormalities, acute myeloid leukaemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A, acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL

3087 clinical trials for this condition and its sub-types, 11 tagged with Acute myeloid leukemia with 11q23 abnormalities itself.

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